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Published in 2020 at "American Journal of Hematology"
DOI: 10.1002/ajh.25999
Abstract: Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant clonal plasma cell disorder, with a 1% yearly risk of progression to multiple myeloma (MM). Evolution of M‐spike and serum free light chain (sFLC) during follow‐up… read more here.
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Published in 2021 at "American Journal of Hematology"
DOI: 10.1002/ajh.26155
Abstract: Despite the benign nature of monoclonal gammopathy of undetermined significance (MGUS), mounting data are associating MGUS with the development of organ dysfunction, specifically monoclonal gammopathy of renal significance (MGRS) and monoclonal gammopathy of neurological significance… read more here.
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Published in 2022 at "Hematological Oncology"
DOI: 10.1002/hon.2992
Abstract: Understanding the progression of monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) is needed to identify patients who would benefit from closer clinical surveillance. Given that two of the defining criteria of MM… read more here.
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Published in 2022 at "Hematological oncology"
DOI: 10.1002/hon.3085
Abstract: 2-[18 F]-FDG PET/CT is a useful diagnostic technique to assess bone and soft tissue disease in multiple myeloma but is not recommended by the International Myeloma Working Group for the evaluation of monoclonal gammopathy of… read more here.
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Published in 2019 at "Annals of Hematology"
DOI: 10.1007/s00277-019-03786-9
Abstract: Dear Editor, The association between plasma cell (PC) neoplasms (PCN) and neutrophilia is a rare but well-known phenomenon [1–3]. CHIP designates asymptomatic presence of clones in the peripheral blood and/or the bone marrow carrying somatic… read more here.
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Published in 2018 at "European Journal of Pediatrics"
DOI: 10.1007/s00431-018-3189-8
Abstract: Approximately 500 cases of idiopathic systemic capillary leak syndrome (Clarkson syndrome) have been reported worldwide. This life-threatening condition is characterized by episodes of increase in vascular permeability with loss of fluid into the interstitium and… read more here.
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Published in 2022 at "Wiener klinische Wochenschrift"
DOI: 10.1007/s00508-022-02012-3
Abstract: Acquired von Willebrand syndrome is exceedingly rare and accounts for only 1–3% of von Willebrand disease cases. In this short report, we present our own cases of acquired von Willebrand syndrome associated with monoclonal gammopathy.… read more here.
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Published in 2018 at "Clinical Rheumatology"
DOI: 10.1007/s10067-018-4064-8
Abstract: To analyze the clinical spectrum, laboratory characteristics, and outcomes of monoclonal gammopathy (MG) in patients with rheumatic diseases. Screening for the presence of MG was performed in 872 inpatients with rheumatic diseases from January 2010… read more here.
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Published in 2020 at "Clinical Rheumatology"
DOI: 10.1007/s10067-020-05501-w
Abstract: Schnitzler’s syndrome (SchS) is a rare autoinflammatory disorder characterized by urticarial rash and monoclonal gammopathy which is currently regarded as IL-1 mediated disease. We present the case of a 21-year-old woman presenting with urticarial rash,… read more here.
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Published in 2021 at "Clinical Rheumatology"
DOI: 10.1007/s10067-020-05565-8
Abstract: To the editor I read with great interest the article by Bixio et al. [1] describing a 21-year-old female with clinically suspected Schnitzler syndrome but without detectable monoclonal gammopathy. In view of her favorable therapeutic… read more here.
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Published in 2021 at "Chinese Journal of Integrative Medicine"
DOI: 10.1007/s11655-021-3446-y
Abstract: Monoclonal gammopathy of renal significance (MGRS) is a pathological state which presents with a spectrum of renal lesions. MGRS is characterized by pathogenic monoclonal immunoglobulins or light chains produced by a premalignant plasma cell or… read more here.